Electrospun nanofiber scaffolds loaded with copper oxide for repairing traumatic brain injury through restoring copper homeostasis and regulating pyroptosis pathway

Yumei An , Sunao Li , Xinqi Huang , Xueshi Chen , Mingyuan Xu , Chen Chen , Xuefeng Zhou , Haiyan Shan , Luyang Tao , Mingyang Zhang

Burns & Trauma ›› 2025, Vol. 13 ›› Issue (1) : tkaf030

PDF (2560KB)
Burns & Trauma ›› 2025, Vol. 13 ›› Issue (1) :tkaf030 DOI: 10.1093/burnst/tkaf030
Research Article
research-article
Electrospun nanofiber scaffolds loaded with copper oxide for repairing traumatic brain injury through restoring copper homeostasis and regulating pyroptosis pathway
Author information +
History +
PDF (2560KB)

Abstract

Background: Traumatic brain injury (TBI) is one of the leading causes of injury and disability worldwide. Pyroptosis, a specific type of programmed cell death (PCD) triggered by inflammatory signals, plays a significant part in the pathological process after TBI. Copper ions play an important role in anti-inflammation and anti-oxidative stress. There is a more active copper metabolism in neurons after injury, and that neurons may require more copper ions and downstream copper-based enzymes to maintain normal physiological functions. Given these understandings of the roles of pyroptosis and copper ions in TBI pathology, this study aims to elucidate the interplay between copper ions and pyroptosis following TBI, with the goal of identifying novel therapeutic targets for TBI management. Methods: We developed an electrostatic spinning scaffold loaded with copper oxide (CuO@PCL/gelatiin, CuO@PG) to achieve small-dose local administration and avoid toxic side effects. The membranes underwent preparation and characterization through various techniques including Fourier transform infrared spectroscopy, measurement of water contact angle, antibacterial experiment, scanning electron microscopy, and assessment of in vitro release of copper. In addition, we used a controlled cortical impact to establish a TBI model in mice to examine the effect of CuO@PG on TBI-induced pyroptosis and the ability of the membranes to heal brain injury. Results: CuO@PG inhibited TBI-induced neuronal pyroptosis. CuO@PG can inhibit the expression of the pyroptosis-related proteins. Moreover, CuO@PG also alleviates brain edema and the degree of neurodegeneration in the acute phase of TBI. The neuroprotective effect of CuO@PG was further confirmed by wire-grip test, open field test, Morris water maze test. Lastly, the beneficial results were significantly inhibited by the use of the copper chelator tetrathiomolybdate. Conclusions: In this study, we successfully constructed electrostatically spun scaffolds loaded with copper oxide to achieve slow, continuous and low-dose copper supply to the local brain, which provides a new theoretical basis for the imbalance of copper homeostasis in the brain after TBI.

Keywords

Traumatic brain injury / Electrospun scaffold / Copper homeostasis / Pyroptosis / Neuroprotection

Cite this article

Download citation ▾
Yumei An, Sunao Li, Xinqi Huang, Xueshi Chen, Mingyuan Xu, Chen Chen, Xuefeng Zhou, Haiyan Shan, Luyang Tao, Mingyang Zhang. Electrospun nanofiber scaffolds loaded with copper oxide for repairing traumatic brain injury through restoring copper homeostasis and regulating pyroptosis pathway. Burns & Trauma, 2025, 13 (1) : tkaf030 DOI:10.1093/burnst/tkaf030

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Maas AIR, Menon DK, Adelson PD, Andelic N, Bell MJ, Belli A, et al. Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research. Lancet Neurol. 2017; 16: 987-1048. https://doi.org/10.1016/S1474-4422(17)30371-X

[2]

Pattinson CL, Gill JM. Risk of dementia after tbi-a cause of growing concern. Nat Rev Neurol. 2018; 14: 511-2. https://doi.org/10.1038/s41582-018-0041-8

[3]

Shi J, Gao W, Shao F. Pyroptosis: Gasdermin-mediated programmed necrotic cell death. Trends Biochem Sci. 2017; 42: 245-54. https://doi.org/10.1016/j.tibs.2016.10.004

[4]

Hu X, Chen H, Xu H, Wu Y, Wu C, Jia C, et al. Role of pyroptosis in traumatic brain and spinal cord injuries. Int J Biol Sci. 2020; 16: 2042-50. https://doi.org/10.7150/ijbs.45467

[5]

Chen X, Huang X, Liu C, Li S, Yang Z, Zhang F, et al. Surface-fill h2s-releasing silk fibroin hydrogel for brain repair through the repression of neuronal pyroptosis. Acta Biomater. 2022; 154: 259-74. https://doi.org/10.1016/j.actbio.2022.11.021

[6]

Ruiz LM, Libedinsky A, Elorza AA. Role of copper on mitochondrial function and metabolism. Front Mol Biosci. 2021; 8: 711227. https://doi.org/10.3389/fmolb.2021.711227

[7]

Shin LJ, Lo JC, Yeh KC. Copper chaperone antioxidant protein1 is essential for copper homeostasis. Plant Physiol. 2012; 159: 1099-110. https://doi.org/10.1104/pp.112.195974

[8]

Urso E, Maffia M. Behind the link between copper and angiogenesis: established mechanisms and an overview on the role of vascular copper transport systems. J Vasc Res. 2015; 52: 172-96. https://doi.org/10.1159/000438485

[9]

Opazo CM, Greenough MA, Bush AI. Copper: from neurotransmission to neuroproteostasis. Front Aging Neurosci. 2014; 6: 143. https://doi.org/10.3389/fnagi.2014.00143

[10]

Blades B, Ayton S, Hung YH, Bush AI, La Fontaine S. Copper and lipid metabolism: a reciprocal relationship. Biochim Biophys Acta Gen Subj. 2021; 1865: 129979. https://doi.org/10.1016/j.bbagen.2021.129979

[11]

Wiriyasermkul P, Moriyama S, Nagamori S. Membrane transport proteins in melanosomes: regulation of ions for pigmentation. Biochim Biophys Acta Biomembr. 2020; 1862: 183318. https://doi.org/10.1016/j.bbamem.2020.183318

[12]

Shawki A, Anthony SR, Nose Y, Engevik MA, Niespodzany EJ, Barrientos T, et al. Intestinal dmt1 is critical for iron absorption in the mouse but is not required for the absorption of copper or manganese. Am J Physiol Gastrointest Liver Physiol. 2015; 309: G635-47. https://doi.org/10.1152/ajpgi.00160.2015

[13]

Ohgami RS, Campagna DR, McDonald A, Fleming MD. The steap proteins are metalloreductases. Blood. 2006; 108: 1388-94. https://doi.org/10.1182/blood-2006-02-003681

[14]

Wong PC, Waggoner D, Subramaniam JR, Tessarollo L, Bartnikas TB, Culotta VC, et al. Copper chaperone for superoxide dismutase is essential to activate mammalian cu/zn superoxide dismutase. Proc Natl Acad Sci USA. 2000; 97: 2886-91. https://doi.org/10.1073/pnas.040461197

[15]

Palumaa P, Kangur L, Voronova A, Sillard R. Metal-binding mechanism of cox17, a copper chaperone for cytochrome c oxidase. Biochem J. 2004; 382: 307-14. https://doi.org/10.1042/BJ20040360

[16]

Petris MJ, Mercer JF, Culvenor JG, Lockhart P, Gleeson PA, Camakaris J. Ligand-regulated transport of the menkes copper p-type atpase efflux pump from the golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking. EMBO J. 1996; 15: 6084-95. https://doi.org/10.1002/j.1460-2075.1996.tb00997.x

[17]

Pilankatta R, Lewis D, Inesi G. Involvement of protein kinase d in expression and trafficking of atp7b (copper atpase). J Biol Chem. 2011; 286: 7389-96. https://doi.org/10.1074/jbc.M110.171454

[18]

Cobbold C, Ponnambalam S, Francis MJ, Monaco AP.Novel membrane traffic steps regulate the exocytosis of the menkes disease atpase. Hum Mol Genet. 2002; 11: 2855-66. https://doi.org/10.1093/hmg/11.23.2855

[19]

Zheng W, Monnot AD. Regulation of brain iron and copper homeostasis by brain barrier systems: implication in neurodegenerative diseases. Pharmacol Ther. 2012; 133: 177-88. https://doi.org/10.1016/j.pharmthera.2011.10.006

[20]

Portbury SD, Hare DJ, Sgambelloni C, Finkelstein DI, Adlard PA. A time-course analysis of changes in cerebral metal levels following a controlled cortical impact. Metallomics. 2016; 8: 193-200. https://doi.org/10.1039/c5mt00234f

[21]

Malikmammadov E, Tanir TE, Kiziltay A, Hasirci V, Hasirci N. Pcl and pcl-based materials in biomedical applications. J Biomater Sci Polym Ed. 2018; 29: 863-93. https://doi.org/10.1080/09205063.2017.1394711

[22]

Siddiqui N, Asawa S, Birru B, Baadhe R, Rao S. Pcl-based composite scaffold matrices for tissue engineering applications. Mol Biotechnol. 2018; 60: 506-32. https://doi.org/10.1007/s12033-018-0084-5

[23]

Fee T, Surianarayanan S, Downs C, Zhou Y, Berry J. Nanofiber alignment regulates nih3t3 cell orientation and cytoskeletal gene expression on electrospun pcl+gelatin nanofibers. PLoS One. 2016; 11: e0154806. https://doi.org/10.1371/journal.pone.0154806

[24]

Rajasekar M, Lavanya M. Gel scaffolds and emerging applications in biomedicine. RSC Adv. 2022; 12: 15925-49. https://doi.org/10.1039/d2ra00924b

[25]

Sheng D, Li J, Ai C, Feng S, Ying T, Liu X, et al. Electrospun pcl/gel-aligned scaffolds enhance the biomechanical strength in tendon repair. J Mater Chem B. 2019; 7: 4801-10. https://doi.org/10.1039/c9tb00837c

[26]

Lu X, Zou H, Liao X, Xiong Y, Hu X, Cao J, et al. Construction of pcl-collagen@pcl@pcl-gelatin three-layer small diameter artificial vascular grafts by electrospinning. Biomed Mater. 2022; 18: 18. https://doi.org/10.1088/1748-605X/aca269

[27]

Suarez DF, Pinzon-Garcia AD, Sinisterra RD, Dussan A, Mesa F, Ramirez-Clavijo S. Uniaxial and coaxial nanofibers pcl/alginate or pcl/gelatine transport and release tamoxifen and curcumin affecting the viability of mcf7 cell line. Nanomaterials (Basel). 2022; 12: 3348. https://doi.org/10.3390/nano12193348

[28]

Chen X, Gao C, Yn Y, Cheng Z, Chen G, Rui T, et al. Ruxolitinib exerts neuroprotection via repressing ferroptosis in a mouse model of traumatic brain injury. Exp Neurol. 2021; 342: 113762. https://doi.org/10.1016/j.expneurol.2021.113762

[29]

Liu W, Chen Y, Meng J, Wu M, Bi F, Chang C, et al. Ablation of caspase-1 protects against tbi-induced pyroptosis in vitro and in vivo. J Neuroinflammation. 2018; 15: 48. https://doi.org/10.1186/s12974-018-1083-y

[30]

Ooigawa H, Nawashiro H, Fukui S, Otani N, Osumi A, Toyooka T, et al. The fate of nissl-stained dark neurons following traumatic brain injury in rats: difference between neocortex and hippocampus regarding survival rate. Acta Neuropathol. 2006; 112: 471-81. https://doi.org/10.1007/s00401-006-0108-2

[31]

Ekici S, Turkarslan S, Pawlik G, Dancis A, Baliga NS, Koch HG, et al. Intracytoplasmic copper homeostasis controls cytochrome c oxidase production. MBio. 2014; 5: e01055-13. https://doi.org/10.1128/mBio.01055-13

[32]

Hellman NE, Gitlin JD. Ceruloplasmin metabolism and function. Annu Rev Nutr. 2002; 22: 439-58. https://doi.org/10.1146/annurev.nutr.22.012502.114457

[33]

An Y, Li S, Huang X, Chen X, Shan H, Zhang M. The role of copper homeostasis in brain disease. Int J Mol Sci. 2022; 23: 23. https://doi.org/10.3390/ijms232213850

[34]

Juan SMA, Daglas M, Gunn AP, Lago L, Adlard PA. Characterization of the spatial distribution of metals and profile of metalloprotein complexes in a mouse model of repetitive mild traumatic brain injury. Metallomics: Integrated Biometal Science. 2022; 14:mfac092. https://doi.org/10.1093/mtomcs/mfac092

[35]

Peng F, Muzik O, Gatson J, Kernie SG, Diaz-Arrastia R. Assessment of traumatic brain injury by increased 64cu uptake on 64cucl2 pet/ct. Journal of Nuclear Medicine: Official Publication, Society of Nuclear Medicine. 2015; 56: 1252-7. https://doi.org/10.2967/jnumed.115.154575

[36]

Petris MJ, Strausak D, Mercer JF. The menkes copper transporter is required for the activation of tyrosinase. Hum Mol Genet. 2000; 9: 2845-51. https://doi.org/10.1093/hmg/9.19.2845

[37]

Gerbasi V, Lutsenko S, Lewis EJ. A mutation in the atp7b copper transporter causes reduced dopamine beta-hydroxylase and norepinephrine in mouse adrenal. Neurochem Res. 2003; 28: 867-73. https://doi.org/10.1023/A:1023219308890

[38]

Qin Z, Itoh S, Jeney V, Ushio-Fukai M, Fukai T. Essential role for the menkes atpase in activation of extracellular superoxide dismutase: implication for vascular oxidative stress. FASEB Journal: Official Publication of the Federation of American Societies For Experimental Biology. 2006; 20: 334-6. https://doi.org/10.1096/fj.05-4564fje

[39]

Steveson TC, Ciccotosto GD, Ma XM, Mueller GP, Mains RE, Eipper BA. Menkes protein contributes to the function of peptidylglycine alpha-amidating monooxygenase. Endocrinology. 2003; 144: 188-200. https://doi.org/10.1210/en.2002-220716

[40]

Shanbhag V, Jasmer-McDonald K, Zhu S, Martin AL, Gudekar N, Khan A, et al. Atp7a delivers copper to the lysyl oxidase family of enzymes and promotes tumorigenesis and metastasis. Proc Natl Acad Sci USA. 2019; 116: 6836-41. https://doi.org/10.1073/pnas.1817473116

[41]

Zirngibl M, Assinck P, Sizov A, Caprariello AV, Plemel JR. Oligodendrocyte death and myelin loss in the cuprizone model: An updated overview of the intrinsic and extrinsic causes of cuprizone demyelination. Mol Neurodegener. 2022; 17: 34. https://doi.org/10.1186/s13024-022-00538-8

[42]

Shin SS, Bray ER, Zhang CQ, Dixon CE. Traumatic brain injury reduces striatal tyrosine hydroxylase activity and potassium-evoked dopamine release in rats. Brain Res. 2011; 1369: 208-15. https://doi.org/10.1016/j.brainres.2010.10.096

[43]

Wasinski F, Pedroso JAB, Dos Santos WO, Furigo IC, Garcia-Galiano D, Elias CF, et al. Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback. J Neurosci. 2020; 40: 4309-22. https://doi.org/10.1523/JNEUROSCI.2531-19.2020

[44]

Michinaga S, Koyama Y. Pathophysiological responses and roles of astrocytes in traumatic brain injury. Int J Mol Sci. 2021; 22: 22. https://doi.org/10.3390/ijms22126418

[45]

Kaler SG. Atp7a-related copper transport diseases-emerging concepts and future trends. Nat Rev Neurol. 2011; 7: 15-29. https://doi.org/10.1038/nrneurol.2010.180

[46]

Xue Q, Kang R, Klionsky DJ, Tang D, Liu J, Chen X. Copper metabolism in cell death and autophagy. Autophagy. 2023; 19: 2175-95. https://doi.org/10.1080/15548627.2023.2200554

[47]

Das A, Ash D, Fouda AY, Sudhahar V, Kim YM, Hou Y, et al. Cysteine oxidation of copper transporter ctr1 drives vegfr2 signalling and angiogenesis. Nat Cell Biol. 2022; 24: 35-50. https://doi.org/10.1038/s41556-021-00822-7

[48]

Zhao Z, Zhou Y, Tian Y, Li M, Dong JF, Zhang J. Cellular microparticles and pathophysiology of traumatic brain injury. Protein & Cell. 2017; 8: 801-10. https://doi.org/10.1007/s13238-017-0414-6

[49]

Iyer SS, He Q, Janczy JR, Elliott EI, Zhong Z, Olivier AK, et al. Mitochondrial cardiolipin is required for nlrp3 inflammasome activation. Immunity. 2013; 39: 311-23. https://doi.org/10.1016/j.immuni.2013.08.001

[50]

Jorgensen I, Miao EA. Pyroptotic cell death defends against intracellular pathogens. Immunol Rev. 2015; 265: 130-42. https://doi.org/10.1111/imr.12287

[51]

Bellouard M, de la GrandMaison GL, Cappy J, Grimaldi L, Lontsi-Djeagou A, Alvarez JC. Trace elements repartition in body fluids, hair and organs in an autopsied population evaluated by icp-ms high resolution. Environ Toxicol Pharmacol. 2022; 95: 103978. https://doi.org/10.1016/j.etap.2022.103978

[52]

Vasilyev VB. Interactions of caeruloplasmin with other proteins participating in inflammation. Biochem Soc Trans. 2010; 38: 947-51. https://doi.org/10.1042/BST0380947

[53]

Dash PK, Redell JB, Hergenroeder G, Zhao J, Clifton GL, Moore A. Serum ceruloplasmin and copper are early biomarkers for traumatic brain injury-associated elevated intracranial pressure. J Neurosci Res. 2010; 88: 1719-26. https://doi.org/10.1002/jnr.22336

[54]

Huuskonen MT, Tuo QZ, Loppi S, Dhungana H, Korhonen P, McInnes LE, et al. The copper bis(thiosemicarbazone) complex cuii(atsm) is protective against cerebral ischemia through modulation of the inflammatory milieu. Neurotherapeutics: the Journal of the American Society For Experimental NeuroTherapeutics. 2017; 14: 519-32. https://doi.org/10.1007/s13311-016-0504-9

[55]

Roberts BR, Lim NKH, McAllum EJ, Donnelly PS, Hare DJ, Doble PA, et al. Oral treatment with cu(ii)(atsm) increases mutant sod1 in vivo but protects motor neurons and improves the phenotype of a transgenic mouse model of amyotrophic lateral sclerosis. J Neurosci. 2014; 34: 8021-31. https://doi.org/10.1523/JNEUROSCI.4196-13.2014

[56]

Pohanka M. Copper and copper nanoparticles toxicity and their impact on basic functions in the body. Bratislavske Lekarske Listy. 2019; 120: 397-409. https://doi.org/10.4149/BLL_2019_065

[57]

Choi BS, Zheng W. Copper transport to the brain by the blood-brain barrier and blood-csf barrier. Brain Res. 2009; 1248: 14-21. https://doi.org/10.1016/j.brainres.2008.10.056

[58]

Uriu-Adams JY, Keen CL. Copper, oxidative stress, and human health. Mol Asp Med. 2005; 26: 268-98. https://doi.org/10.1016/j.mam.2005.07.015

[59]

Chen Y, Saari JT, Kang YJ. Weak antioxidant defenses make the heart a target for damage in copper-deficient rats. Free Radic Biol Med. 1994; 17: 529-36. https://doi.org/10.1016/0891-5849(94)90092-2

[60]

Pavlovic D, Pekic S, Stojanovic M, Popovic V. Traumatic brain injury: neuropathological, neurocognitive and neurobehavioral sequelae. Pituitary. 2019; 22: 270-82. https://doi.org/10.1007/s11102-019-00957-9

[61]

Isaev NK, Stelmashook EV, Genrikhs EE. Role of zinc and copper ions in the pathogenetic mechanisms of traumatic brain injury and alzheimer’s disease. Rev Neurosci. 2020; 31: 233-43. https://doi.org/10.1515/revneuro-2019-0052

[62]

Sharma R, Kambhampati SP, Zhang Z, Sharma A, Chen S, Duh EI, et al. Dendrimer mediated targeted delivery of sinomenine for the treatment of acute neuroinflammation in traumatic brain injury. Journal of Controlled Release: Official Journal of the Controlled Release Society. 2020; 323: 361-75. https://doi.org/10.1016/j.jconrel.2020.04.036

[63]

Zhong CC, Zhao T, Hogstrand C, Chen F, Song CC, Luo Z. Copper (cu) induced changes of lipid metabolism through oxidative stress-mediated autophagy and nrf2/pparγ pathways. J Nutr Biochem. 2022; 100: 108883. https://doi.org/10.1016/j.jnutbio.2021.108883

[64]

van Hameren G, Muradov J, Minarik A, Aboghazleh R, Orr S, Cort S, et al. Mitochondrial dysfunction underlies impaired neurovascular coupling following traumatic brain injury. Neurobiol Dis. 2023; 186: 106269. https://doi.org/10.1016/j.nbd.2023.106269

[65]

Donnelly PS, Xiao Z, Wedd AG.Copper and alzheimer’s disease. Curr Opin Chem Biol. 2007; 11: 128-33. https://doi.org/10.1016/j.cbpa.2007.01.678

[66]

Singh SK, Balendra V, Obaid AA, Esposto J, Tikhonova MA, Gautam NK, et al. Copper-mediated β-amyloid toxicity and its chelation therapy in alzheimer’s disease. Metallomics: Integrated Biometal Science. 2022; 14: mfac018. https://doi.org/10.1093/mtomcs/mfac018

[67]

Yang M, Wu X, Hu J, Wang Y, Wang Y, Zhang L, et al. Commd10 inhibits hif1α/cp loop to enhance ferroptosis and radiosensitivity by disrupting cu-fe balance in hepatocellular carcinoma. J Hepatol. 2022; 76: 1138-50. https://doi.org/10.1016/j.jhep.2022.01.009

PDF (2560KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉